Canonical Allele Identifier: CA367582483

Gene: EGFR

Linked Data

• MyVariant Identifiers: chr7:g.55268949A>C (hg19) ; chr7:g.55201256A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.55201256A>C , CM000669.2:g.55201256A>C	GRCh38
NC_000007.13:g.55268949A>C , CM000669.1:g.55268949A>C	GRCh37
NC_000007.12:g.55236443A>C	NCBI36
NG_007726.3:g.187225A>C , LRG_304:g.187225A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450046.2:c.2856A>C	ENSP00000413354.2:p.Glu952Asp
ENST00000700145.1:c.900-4091A>C
ENST00000700146.1:n.759A>C
ENST00000700147.1:n.684A>C
ENST00000275493.7:c.3015A>C MANE Select	ENSP00000275493.2:p.Glu1005Asp
ENST00000275493.6:c.3015A>C	ENSP00000275493.2:p.Glu1005Asp
ENST00000442591.5:c.*28+28328A>C	ENSP00000410031.1:n.*28+28328A>C
ENST00000454757.6:c.2880A>C	ENSP00000395243.3:p.Glu960Asp
ENST00000455089.5:c.2880A>C	ENSP00000415559.1:p.Glu960Asp
NM_005228.3:c.3015A>C , LRG_304t1:c.3015A>C	NP_005219.2:p.Glu1005Asp
NM_001346897.1:c.2880A>C	NP_001333826.1:p.Glu960Asp
NM_001346898.1:c.3015A>C	NP_001333827.1:p.Glu1005Asp
NM_001346899.1:c.2880A>C	NP_001333828.1:p.Glu960Asp
NM_001346900.1:c.2856A>C	NP_001333829.1:p.Glu952Asp
NM_001346941.1:c.2214A>C	NP_001333870.1:p.Glu738Asp
NM_005228.4:c.3015A>C	NP_005219.2:p.Glu1005Asp
NM_005228.5:c.3015A>C MANE Select	NP_005219.2:p.Glu1005Asp
NM_001346897.2:c.2880A>C	NP_001333826.1:p.Glu960Asp
NM_001346898.2:c.3015A>C	NP_001333827.1:p.Glu1005Asp
NM_001346900.2:c.2856A>C	NP_001333829.1:p.Glu952Asp
NM_001346941.2:c.2214A>C	NP_001333870.1:p.Glu738Asp
NM_001346899.2:c.2880A>C	NP_001333828.1:p.Glu960Asp